EP3065665B1 - Emballages à éléments multiples pour dispositifs médicaux - Google Patents

Emballages à éléments multiples pour dispositifs médicaux Download PDF

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Publication number
EP3065665B1
EP3065665B1 EP14795923.3A EP14795923A EP3065665B1 EP 3065665 B1 EP3065665 B1 EP 3065665B1 EP 14795923 A EP14795923 A EP 14795923A EP 3065665 B1 EP3065665 B1 EP 3065665B1
Authority
EP
European Patent Office
Prior art keywords
tray
retainer
medical device
package
distal end
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP14795923.3A
Other languages
German (de)
English (en)
Other versions
EP3065665A1 (fr
Inventor
Denise Marie Dacey
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ethicon LLC
Original Assignee
Ethicon LLC
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Filing date
Publication date
Application filed by Ethicon LLC filed Critical Ethicon LLC
Publication of EP3065665A1 publication Critical patent/EP3065665A1/fr
Application granted granted Critical
Publication of EP3065665B1 publication Critical patent/EP3065665B1/fr
Active legal-status Critical Current
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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B50/00—Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B50/00—Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers
    • A61B50/10—Furniture specially adapted for surgical or diagnostic appliances or instruments
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B50/00—Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers
    • A61B50/30—Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B50/00—Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers
    • A61B50/30—Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments
    • A61B50/33—Trays
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B50/00—Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers
    • A61B2050/005—Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers with a lid or cover
    • A61B2050/0058—Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers with a lid or cover closable by translation
    • A61B2050/006—Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers with a lid or cover closable by translation perpendicular to the lid plane, e.g. by a downward movement
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B50/00—Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers
    • A61B2050/005—Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers with a lid or cover
    • A61B2050/0067—Types of closures or fasteners
    • A61B2050/0068—Cooperating dimples
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B50/00—Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers
    • A61B50/30—Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments
    • A61B2050/314—Flexible bags or pouches

Definitions

  • the present invention is generally related to medical devices, and is more specifically related to packages for medical devices.
  • An operating team typically includes at least one member whose primary function is to open packages containing medical devices and to present the medical devices to a sterile nurse or surgeon in a manner that maintains the medical devices in a sterile condition.
  • the package must properly surround and protect the medical device from damage.
  • the packaging materials must be chosen to accommodate the sterilization process that will be used for the medical device.
  • the package must be easy to open to enable efficient access of the medical device during a surgical procedure.
  • Packages for medical devices are also subject to considerations such as the cost of the materials, the cost and complexity of tooling to make the package, ease of package assembly, and ease of manufacture and shipping both the empty package and after the components are assembled together.
  • An increasingly competitive economic environment exacerbates these sometimes competing considerations so that safety and efficacy must be achieved while costs are minimized.
  • One type of package provides a color-marked envelope that indicates the area to be torn off to provide an access opening to the contents within the envelope without affecting the sterility of the contents.
  • Another type of package provides a tear string that may be pulled to open the envelope so that the contents may be removed using forceps or similar tools.
  • U. S. Pub. No. 2003/0121821 concerns a kit which includes a blister tray and a package for a small device insertable within the blister tray.
  • U. S. Pub. No. 2012/0061262 concerns a package for a medical device having a handle and an elongated shaft which includes a holster for the medical device.
  • U. S. Pat. No. 5,972,008 concerns a retaining apparatus for a surgical mesh which includes a top surface and a bottom surface.
  • a sealed pouch includes first and second foil sheets having opposing inner surfaces that are joined together by a seal for defining a sealed area of the pouch located inside the seal and an unsealed area of the pouch located outside the seal.
  • the sealed pouch includes a textured opening flange located adjacent an edge of the pouch for peeling the first and second foil sheets away from one another for breaking the seal and opening the sealed pouch.
  • the textured opening flange is located within the unsealed area of the pouch and includes at least one roughened surface formed on at least one of the first and second foil sheets.
  • a leg of the seal passes through the textured opening flange. The roughened surface on the textured opening flange makes it easier to break the leg of the seal for pulling the foil sheets apart.
  • a package for a medical device desirably includes a tray having proximal and distal ends, top and bottom surfaces, lateral retention elements, and proximal and distal retention elements, and a proximal retainer sleeve fastened to a proximal section of the tray that covers the top surface of the tray.
  • the retainer sleeve preferably has a section that can be rotationally displaced to expose a portion of a medical device disposed on the tray and to allow the medical device to be removed from the tray by rotating a proximal end of the medical device and, after the proximal end is clear of proximal retention elements, moving the medical device in a proximal direction to remove the device from the proximal end of the tray.
  • the package of the present invention may be used in a method of dispensing a medical device from a medical device package, which preferably includes grasping the medical device located at the proximal end of the tray, rotating the medical device sufficiently to enable one side of the medical device to clear at least one retention element, and moving the medical device in a proximal direction away from the medical device package until the medical device is completely disengaged from the medical device package.
  • a package for a medical device includes a tray having a top surface, a bottom surface, a proximal end, a distal end, and first and second lateral sides that extend between the proximal and distal ends.
  • the tray desirably has molded elements projecting from the top surface.
  • the package includes a retainer lid secured to the tray for covering the top surface of the tray at the distal end of the tray, and optionally a retainer sleeve having a distal end and a proximal end. The distal end of the retainer sleeve is wrapped around the top and bottom surfaces of the tray and is secured to the tray by the retainer lid.
  • the proximal end of the retainer sleeve includes a top panel that covers the top surface of the tray at the proximal end of the tray.
  • the top panel of the retainer sleeve has a free edge that is adapted to flex away from the top surface of the tray to provide access to the medical device.
  • the retainer sleeve includes a cut that extends between the free edge of the top panel and the distal end of the retainer sleeve for enabling the free edge of the top panel to move relative to the distal end of the retainer sleeve.
  • the tray is made of a polymer material.
  • the tray is thermoformed and is made of high-density polyethylene (HDPE).
  • the molded elements of the tray preferably define a first channel adjacent the proximal end of the tray, a second channel distal to the first channel that extends toward the distal end of the tray, and at least one retaining element located at the proximal end of the tray.
  • the at least one retaining element includes a pair of retainer posts that are spaced from one another at the proximal end of the tray. When the medical device is loaded onto the tray, the retainer posts prevent proximal movement of the medical device relative to the tray.
  • the molded elements on the tray desirably include a mound located between the first and second channels.
  • the mound preferably has a top surface including a flat proximal section and a sloping distal section that slopes downwardly toward the distal end of the tray.
  • the first and second channels desirably intersect one another at the mound.
  • the first and second channels define recesses molded into the tray and the mound projects above the recesses of the first and second channels.
  • the mound has a proximal face that opposes the first and second retainer posts. A handle of a medical device is disposed between the retainer posts and the proximal face of the mound, which prevents proximal and distal movement of the medical device relative to the tray.
  • the top surface of the tray preferably includes a central depression that extends between the proximal edge of the tray and the proximal face of the mound.
  • the central depression is desirably located between the first and second retainer posts.
  • the medical device preferably has a handle and an elongated shaft extending from the handle.
  • the handle is preferably disposed in the first channel of the tray and the elongated shaft is preferably disposed in the second channel of the tray.
  • the top panel of the retainer sleeve preferably covers the handle of the medical device. The cut formed in the retainer sleeve desirably enables the free edge of the top panel to be flexed away from the handle and the top surface of the tray to allow access to and removal of the medical device from the tray.
  • the top surface of the tray preferably has one or more snap-fit depressions molded therein at the distal end of the tray and the retainer lid has one or more snap-fit projections molded therein that extend from a bottom surface thereof.
  • the one or more snap-fit projections of the retainer lid are preferably insertable into the one or more snap-fit depressions of the tray for securing the retainer lid to the tray.
  • the distal end of the retainer sleeve desirably has one or more cutouts that are aligned with at least one of the one or more snap-fit depressions molded in the tray.
  • at least one of the one or more snap-fit projections on the retainer lid pass through the one or more cutouts and into a corresponding snap-fit depression for securing the distal end of the retainer sleeve to the tray.
  • the retainer sleeve preferably includes a bottom panel that is adapted to cover the bottom surface of the tray, a top panel that is attached to a first edge of the bottom panel, and a connecting panel attached to a second edge of the bottom panel.
  • the retainer sleeve is foldable for being wrapped around the tray for covering the top and bottom surfaces and the first and second lateral sides of the tray.
  • the tray preferably includes a polymer material, such as high-density polyethylene (HDPE), the retainer lid desirably includes a polymer material, such as polypropylene (PP), and the retainer sleeve is preferably made of a cellulose material, such as paperboard.
  • the tray is made of HDPE
  • the retainer lid is made of PP
  • the retainer sleeve is paperboard.
  • the tray thins toward the distal end of the tray so that the proximal end of the tray is thicker and the distal end of the tray is thinner.
  • the package desirably includes an outer pouch that receives the package, such as a sealable foil pouch.
  • the outer pouch is adapted to receive the assembled package including the tray, the medical device on the tray, the retainer lid and the retainer sleeve.
  • the tray has a peripheral flange that extends around the outer perimeter of the tray.
  • the flange may include segmented lifts projecting from an underside of the flange.
  • the flange divides the tray into a topside and a bottom side so that the top surface of the tray is located above the peripheral flange and the bottom surface of the tray is located below the peripheral flange.
  • a package for a medical device preferably includes a thermoformed tray having a top surface, a bottom surface, a proximal end, a distal end, and first and second lateral sides that extend between the proximal and distal ends.
  • a medical device is disposed over the top surface of the tray, the medical device having a handle and an elongated shaft projecting from the handle.
  • the tray preferably has molded elements projecting from the top surface including a first channel for receiving the handle, a second channel for receiving the elongated shaft, a mound located between the first and second channels, and a pair of retainer posts located at the proximal end of the tray.
  • the handle is disposed between the retainer posts and the mound for minimizing proximal and distal movement of the medical device relative to the tray.
  • the package preferably includes a thermoformed retainer lid secured to the tray for covering the elongated shaft of the medical device at the distal end of the tray, and a retainer sleeve having a distal end and a proximal end, the distal end of the retainer sleeve being wrapped around the tray to cover the top and bottom surfaces of the tray.
  • the distal end of the retainer sleeve is secured to the tray by the retainer lid.
  • the proximal end of the retainer sleeve desirably includes a top panel that covers the top surface of the tray at the proximal end of the tray.
  • the top panel of the retainer sleeve preferably has a free edge that is adapted to flex away from the top surface of the tray to provide access to the handle of the medical device.
  • the handle preferably has a base and the handle is pivotable about the base to clear the handle of the retainer posts so that the medical device is free to be moved in a proximal direction relative to the tray to remove the medical device from the tray.
  • the tray is thermoformed and is desirably made from HDPE.
  • the tray is inclined so that it is thicker at the proximal end and thinner at the distal end of the device, which minimizes the pouch size while allowing for a smooth seal line to be formed on the foil pouch.
  • the thicker end of the tray is loaded into the pouch so that the thinner end of the tray is adjacent the final seal to be formed for completely sealing the pouch.
  • the bottom surface of the tray preferably has one or more segmented lifts that offset the peripheral flange on the tray from the seal of the outer pouch to minimize the likelihood of the peripheral flange of the tray damaging or compromising the seal of the outer pouch.
  • the segmented lifts also preferably facilitate the flow of sterilization gasses throughout the outer pouch and around the tray, and may also protect the outer pouch from being cut by the peripheral flange of the tray.
  • a package for a medical device desirably includes a tray having a top surface, a bottom surface, a proximal end, a distal end, and first and second lateral sides that extend between the proximal and distal ends.
  • the tray preferably has elements, such as molded elements, projecting from the top surface of the tray for holding a medical device.
  • the package desirably includes a retainer lid secured to the tray for covering the top surface of the tray at the distal end of the tray, and the cover flap having a distal end and a proximal end.
  • a lateral edge of the cover flap is attached to one lateral side of the tray and the distal end of the cover flap is secured to the tray by the retainer lid.
  • the cover flap preferably covers the top surface of the tray at the proximal end of the tray.
  • the cover flap desirably has a free edge that is adapted to flex away from the top surface of the tray for providing access to a medical device loaded on the tray.
  • the tray is formed to accommodate an elongated medical device, such as a medical device having a straight or curved distal portion, e.g., a shaft.
  • an elongated medical device such as a medical device having a straight or curved distal portion, e.g., a shaft.
  • the multi-component package includes a retainer lid that is secured over the top surface of the tray for covering a distal end of the tray.
  • the retainer lid may be snap-fit onto the tray.
  • the distally located retainer lid is made from polypropylene (PP).
  • PP polypropylene
  • both HDPE and PP are hydrophobic materials, which are preferred over other thermoform materials (e.g., PET) for an EtO sterilization process that needs to be vacuum dried before final sealing.
  • Both HDPE and PP are preferred over other thermoform materials such as PET and PVC because the trimmed edges of HDPE and PP thermoform are comparatively not as sharp as other thermoform materials (e.g., PET and PVC).
  • the PP retainer lid is preferably clear so as to provide a visual indication of the presence of the medical device in the tray.
  • the retainer sleeve is not made of paperboard but is made of a clear material such as a flexible, semi-rigid plastic film (e.g., PP).
  • the package may include a desiccant material that is separate from the retainer sleeve.
  • the retainer lid desirably snap fits onto the tray.
  • the retainer lid has snap-fit projections that extend from the bottom surface of the retainer lid that are inserted into corresponding snap-fit depressions formed in the top surface of the tray.
  • a gap is provided between the snap-fit projections on the retainer lid and the corresponding snap-fit depressions on the tray, which facilitates efficient EtO gas infiltration throughout the top and bottom surfaces of the tray.
  • the retainer lid is preferably transparent, which allows for visibility of the medical device within the assembled package.
  • the multi-component package preferably includes a retainer sleeve that is secured to a proximal end of the tray.
  • the retainer sleeve preferably provides a smoothing element that isolates the tray and the medical device from an outer pouch.
  • the retainer sleeve is made of paperboard and serves as a desiccant, which is particularly beneficial for EtO sterilized absorbable products.
  • the paperboard retainer sleeve preferably includes a cut that enables a portion of the retainer sleeve to be flexed away from the top surface of the tray to expose a portion of the medical device, which enables medical personnel to access the medical device and remove the medical device from the package without requiring disassembly of the package.
  • the paperboard sleeve is preferably secured to the tray and the retainer lid by means of a snap-fit connection between the retainer lid and the tray.
  • the retainer sleeve that is secured to the tray by the retainer lid wraps completely around the tray (e.g., 360°).
  • the retainer sleeve covers deep recesses formed in the underside of the tray, which is important during a vacuum drying cycle associated with an EtO sterilization process by keeping the pouch as smooth as possible on both the top surface and bottom surface of the tray.
  • the wrap-around retainer sleeve provides enhanced security by preventing accidental dropping of the medical device while still allowing for an efficient method of dispensing the medical device from the package.
  • the tray, the medical device on the tray, the retainer sleeve and the retainer lid are placed into an outer pouch that may be sealed.
  • the outer dimensions of the tray preferably closely match the seal line of the outer pouch. The close match between the outer perimeter of the tray and the inner seal line of the outer pouch limits movement of the tray relative to the outer pouch, which is especially important during shipping and handling.
  • the tray, the retainer lid, and the retainer sleeve desirably protect the outer pouch from being impacted by the medical device during loading, sterilization, shipping and handling of the package.
  • the tray further protects the medical device by restraining the medical device from moving within the plane of the tray during shipping and handling of the package.
  • the location of an integrated paperboard retainer sleeve allows for one-handed device dispensing.
  • the cut on the paperboard retainer sleeve allows a top panel of the retainer sleeve to be easily flexed, which enables easy access and removal of a medical device from the tray.
  • flexing the retainer sleeve away from the top surface of the tray allows a user to easily grip the handle and rotate the handle away from the top surface of the tray for removing the medical device from the tray.
  • the handle of the medical device may be rotated away from the retaining elements so that the handle is unconstrained by the retainer elements. Once the handle is rotated into a position whereby it is clear of the retainer elements, the handle may be pulled in a proximal direction to remove the medical device from the proximal end of the tray.
  • the retainer lid and the paperboard retainer sleeve may be separated from one another so that the tray, the retainer lid and the retainer sleeve may be recycled.
  • a package 50 for a medical device 52 preferably includes a tray 54 adapted to receive the medical device 52, a retainer lid 56 that is snap-fit onto a distal end of the tray 54, and a retainer sleeve 58, that is wrapped around the proximal end of the tray 54.
  • the retainer sleeve 58 is wrapped around the tray and is secured to the tray by the retainer lid 56.
  • the assembled package 50 may be inserted into an open end of a sealable outer pouch 60, such as a foil pouch.
  • the tray 54 of the package desirably includes a proximal end 62, a distal end 64, a first lateral side 66, and a second lateral side 68.
  • the tray 54 preferably has a peripheral outer flange 70 that extends around the outer perimeter of the tray.
  • the flange 70 preferably divides the tray 54 into a top surface 72 configured to receive a medical device, and a bottom surface 74 that is opposite the top surface 72.
  • the tray 54 is preferably thermoformed and is made of a polymer material such as high-density polyethylene (HDPE).
  • HDPE high-density polyethylene
  • the tray 54 preferably includes a first channel 76 molded into the top surface that is adapted to receive a handle portion of the medical device 52 shown in FIG. 1 of the present application.
  • the tray 54 also desirably includes a second channel 78 molded into the top surface that is adapted to receive the elongated shaft of the medical device 52 ( FIG. 1 ).
  • the first channel 76 desirably includes a centrally located depression 80 bounded on a first side by a first flat surface 82 and a second side by a second flat surface 84.
  • the top surface of the tray at the proximal end 62 thereof is generally open and is not surrounded by vertically extending constraints other than retainer posts as will be further disclosed herein.
  • the first channel 76 also desirably includes a second depression 86 located between the first flat surface 82 and the flange 70 at the outer perimeter of the tray 54.
  • the tray 54 preferably includes a concave- shaped recess 88 located at the distal end of the first channel 76, which is molded into a proximal face of a mound 90 of the tray 54.
  • the mound 90 is located at the distal end of the first channel 76.
  • the mound 90 preferably includes a proximal flat section 92 and a distal sloping section 94 that slopes downwardly toward the distal end 64 of the tray 54. As shown in FIG. 2C , the distal sloping section 94 of the mound 90 slopes downwardly toward the distal end 64 and the bottom side 74 of the tray 54 so that the proximal end of the tray is thicker than the distal end of the tray.
  • the tray 54 also desirably includes the second channel 78 that passes through the mound 90 toward the distal end 64 of the tray.
  • the second channel 78 includes a first wall 96 and an opposing second wall 98.
  • the second channel 78 is designed to receive an elongated shaft of a medical device.
  • the second wall 98 of the second channel 78 has a concave shape that conforms to a curved shape of an elongated shaft of a medical device.
  • the tray 54 desirably includes a pair of spaced retention posts 100, 102 that are located adjacent the proximal end 62 of the tray.
  • the proximally located retention posts 100, 102 are desirably spaced from one another by the central depression 80 formed in the first channel 76 of the tray.
  • the retention posts 100, 102 prevent a medical device loaded onto the tray from sliding and/or moving in a proximal direction relative to the tray.
  • the medical device is constrained from moving toward the proximal end of the tray by the retention posts 100, 102, however, the medical device may be removed from the tray by rotating the handle of the medical device away from the top surface of the tray until the handle is clear of the retention posts 100, 102. Once the handle is clear of the retention posts, the medical device may be pulled in a proximal direction for removing the medical device from the tray.
  • the distal end 64 of the tray 54 preferably includes four snap-fit depressions 104A-104D molded into the top surface of the tray that are adapted to receive similarly shaped projections formed on an underside of the retainer lid 56 ( FIG. 1 ), as will be described in more detail herein.
  • the tray 54 preferably includes a first circulation chamber 106 for circulating EtO gasses, which is located between the first and second snap-fit depressions 104A, 104B, the outer perimeter flange 70 extending along the first lateral side of the tray and the first wall 96 of the second channel 78.
  • the top surface of the tray 54 also desirably includes a second EtO gas circulating chamber 108 that is located between the third and fourth snap-fit depressions 104C, 104D, the outer perimeter flange 70 extending along the second lateral side of the tray and the second wall 98 of the second channel 78.
  • the top side of the tray 54 desirably includes a number of EtO gas circulating grooves formed therein to ensure that the EtO gasses may easily circulate throughout the top surface of the tray.
  • the tray includes a first groove 110 that provides fluid communication between the first snap-fit depression 104A and the first circulation chamber 106, a second groove 112 that provides fluid communication between the first circulation chamber 106 and the second channel 78, and a third groove 114 that provides fluid communication between the second snap-fit depression 104B and the second channel 78.
  • the top surface of the tray 54 also desirably includes a fourth groove 116 that provides fluid communication between the third snap-fit depression 104C and the second channel 78, a fifth groove 118 that provides fluid communication between the fourth snap-fit depression 104D and the second gas circulation channel 108 and a sixth groove 120 that provides fluid communication between the second gas circulation chamber 108 and the second channel 78.
  • the EtO gasses preferably pass through the first channel 76, the second channel 78, the first and second gas circulation chambers 106, 108, and the four snap-fit depressions 104A, 104D via the above described grooves 110-120 molded into the top surface of the tray 54.
  • the tray 54 preferably has a length L 1 of about 30,48- 40,64 cm (12-16 inches) and more preferably about 37,78 cm (14.875 inches), and a width W 1 of about 15,24- 20,32 cm (6-8 inches) and more preferably about 19,32 cm (7.606 inches).
  • the tray 54 preferably includes spacers 122A-122F projecting from the bottom surface of the peripheral flange 70.
  • first and second spacers 122A, 122B extend along the first lateral side 66 of the tray
  • a third spacer 122C extends along the distal end 64 of the tray
  • fourth and fifth spacers 122D, 122E extend along the second lateral side 68 of the tray
  • a sixth spacer 122F extends along the proximal end 62 of the tray. As shown in FIGS.
  • the spacers 122 preferably project from the bottom surface of the flange to lift the flange 70 away from an opposing inner surface of the outer pouch 60 ( FIG. 1 ). Spacing the flange 70 away from the opposing inner surface of the pouch ensures efficient circulation of the EtO gasses around the tray 54 and also ensures that the outer flange 70 will not damage an opposing seal formed in the outer pouch 60.
  • the retention posts 100, 102 and the sixth spacer 122F at the proximal end 64 of the tray define a height H 1 of about 2,54-5,08 cm (1-2 inches) and more preferably about 3,78 cm (1.490 inches).
  • the spacers 122 preferably define a height H 2 between the flange 70 and the lower end of the spacer of about 0,254- 0,508 cm (0.10-0.20 inches) and more preferably about 0,396 cm (0.156 inches).
  • the tray 54 is preferably thicker at the proximal end 62 and thinner at the distal end 64.
  • the tray 54 preferably narrows between the proximal end 62 and the distal end 64 of the tray so that the distal end 64 of the tray is thinner than the proximal end 62 of the tray.
  • the retainer lid 56 preferably includes a top surface 130, a bottom surface 132, and four snap-fit projections 134A-134D that project from the bottom surface 132 thereof.
  • the retainer lid 56 desirably includes a first depression 136 that conforms in size and shape to the first gas circulation chamber 106 in the tray 54 ( FIG. 2B ) and a second depression 138 sized and shaped to conform to the second gas circulation chamber 108 in the tray 54.
  • the first and second depressions 136, 138 project from the bottom surface 132 of the retainer lid 56.
  • each snap-fit projection 134A-134D defines a height H 3 of about 0,762- 0,889 cm ( 0.300-0.350 inches) and more preferably about 0,813 cm (0.320 inches).
  • the retainer lid 56 has a length L 2 of about 12,70- 17,78 cm (5-7 inches) and more preferably about 14,64 cm (5.763 inches). and a width W 2 of about 13,97- 16,51 cm ( 5.5-6.5 inches) and more preferably about 14,20 cm (5.590 inches).
  • the retainer lid 56 is desirably secured over the distal end of the tray 54 ( FIGS. 2A-2D ) for covering a distal end of a medical device ( FIG.1 ) loaded onto the tray.
  • the retainer lid 56 also desirably secures the retainer sleeve to the tray.
  • the retainer sleeve 58 preferably includes a paperboard blank having a top panel 140, a bottom panel 142 and a connecting panel 144.
  • a first fold line 146 desirably extends between the top panel 140 and the bottom panel 142 for facilitating folding of the top panel over the bottom panel.
  • the retainer sleeve 58 desirably includes a second fold line 148 that extends between the bottom panel 142 and the connecting panel 144 for facilitating folding of the bottom panel relative to the connecting panel.
  • the top panel 140 desirably includes a proximal edge 150, a distal edge 152 and an outer edge 154.
  • the top panel 140 desirably includes a cut 156 formed therein that extends from the outer edge 154 toward the first fold line 146.
  • the cut 156 has a length L 3 of about 3,81- 4,45 cm (1.50-1.75 inches) and more preferably about 4,29 cm (1.69 inches).
  • the top panel 140 includes an elongated cutout 158 that extends along the distal edge 152 thereof.
  • the elongated cutout 158 has a length L 4 of about 12,70- 13,97 cm (5.00-5.50 inches) and more preferably about 13,26 cm (5.22 inches) and a width W 3 of about 1,27- 2,54 cm ( 0.50-1.00 inches) and more preferably about 2,21 cm (0.87 inches).
  • a first pair of notches 160A, 160B may be provided at the ends of the first fold line 146 for facilitating folding of the top panel 140 and the bottom panel 142 relative to one another.
  • the retainer sleeve 58 may also include a second pair of notches 162A, 162B provided at the ends of the second fold line 148 for facilitating folding of the bottom panel 142 and the connecting panel 144 relative to one another.
  • the connecting panel 144 desirably includes a proximal edge 164 and a distal edge 166 with a second cutout 168 formed in the connecting panel adjacent the distal edge 166 thereof.
  • the retainer sleeve 58 is folded for being wrapped about the tray 54 shown and described above in FIGS. 2A-2D .
  • the connecting panel 164 is preferably folded over the bottom panel 142 and the top panel 140 is folded over the connecting panel 164.
  • the elongated cutout 158 at the distal end 152 of the top panel 140 is preferably aligned with the second cutout 168 at the distal end 166 of the connecting panel 164.
  • the first snap-fit projection 134A on the retainer lid ( FIG. 3A ) is passed through the aligned elongated cutout 158 and the second cutout 168 for at least partially securing the distal end of the retainer sleeve 58 to the tray 54 ( FIG. 2A ).
  • the tray 54 is configured to receive a medical device, such as an applicator instrument, by placing the tray atop a surface with the top surface of the tray facing away from the surface.
  • a medical device such as an applicator instrument
  • a medical device 52 is placed onto the tray 54 with the handle 53 disposed in the first channel 76 and the curved elongated shaft 65 disposed in the second channel 78.
  • the leading face of the handle 53 opposes the concave shaped cutout 88 formed at the proximal end of the mound 90 and the trailing end of the handle 53 abuts against the first and second retaining posts 100, 102.
  • the handle 53 is constrained from proximal and distal movement relative to the plane of the tray.
  • the retainer lid 56 may be secured over the distal end of the tray 54 by inserting the four snap-fit projections on the retainer lid 56 into the four snap-fit depressions on the tray 54.
  • FIG. 7A the retainer sleeve is not shown so that the position of the medical device 52 and the retainer lid 56 may be clearly displayed.
  • the first and second retaining posts 100, 102 act as stops that prevent proximal movement of the handle 53 of the medical device 52 toward the proximal end 62 of the tray 54.
  • the retainer lid 56 is snap-fit onto the distal end 64 of the tray 54 for covering the elongated shaft of the medical device 52.
  • the central depression 80 formed in the top surface 72 of the tray 54 extends between the first and second retaining posts 100, 102.
  • medical personnel may place a thumb into the central depression 80 and one or more fingers into the concave cutout 88 ( FIG. 7A ) for grasping the handle 53 of the applicator instrument 52 and rotating the handle 53 in the direction indicated by R 1 .
  • the handle 53 is preferably rotated until it clears the retaining posts 100, 102 so that it may be slid proximally toward the proximal end 62 of the tray 54 ( FIG. 7A ) for removing the medical device 52 from the tray.
  • FIG. 8 shows an exploded view of the components of a package 50 for a medical device 52 prior to assembly.
  • the package 50 preferably includes the tray 54 adapted to receive the medical device 52 so that the handle 53 is disposed within the first channel 76 of the tray and the elongated shaft 65 is disposed within the second channel 78 of the tray.
  • the retainer sleeve 58 is preferably wrapped about the proximal end of the tray 54 so that the top panel 140 of the retainer sleeve overlies the top surface 72 of the tray 54 with the elongated cutout 158 of the sleeve aligned with the snap-fit depressions 104A, 104C and the second cutout 168 aligned with the first snap-fit depression 104A.
  • the snap-fit projections 134A on the retainer lid 56 are inserted into the corresponding snap-fit depressions 104-104D on the tray 54 for securing the retainer lid 56 over the distal end of the tray 54.
  • the first snap-fit projection 134A preferably passes through the second cutout 168 and the elongated first cutout 158 of the retainer sleeve 58 and is inserted into the first snap-fit depression 104A
  • the fourth snap-fit projection 134D preferably passes through the elongated cutout 158 of the retainer sleeve 58 and is inserted into the fourth snap-fit depression 104D.
  • the retainer lid 56 both covers the shaft 65 of the medical device 52 that is disposed in the second chamber 78 of the tray, and secures the distal end of the retainer sleeve 58 to the tray.
  • the multi-component package 50 is assembled by placing the medical device 52 on the top surface of the tray 54 so that the handle portion 53 is disposed within the first channel 76 and the elongated shaft 65 is disposed within the second channel 78.
  • the bottom surface of the tray 54 is preferably positioned atop the retainer sleeve 58 with the tray aligned over the bottom panel 142 of the retainer sleeve.
  • the first lateral side 66 of the tray 54 is preferably aligned with the first fold line 146 that extends between the bottom panel 142 and the connecting panel 144.
  • the second lateral side 68 of the tray 54 is preferably aligned with the second fold line 148 extending between the bottom panel 142 and the top panel 140.
  • the connecting panel 144 of the retainer sleeve 58 is folded over the first lateral edge 66 of the tray 54 so that its free end overlies the top surface of the tray 54.
  • the first cutout 168 formed in the connecting panel 144 is preferably aligned with the first snap-fit depression 104A formed in the top surface of the tray 54.
  • the top panel 140 of the retainer sleeve 58 is desirably folded over the second lateral edge 68 of the tray 54 so that it overlies the top surface of the tray.
  • the elongated cutout 158 of the top panel 140 is preferably aligned with the first snap-fit depression 104A and the fourth snap-fit depression 104D provided in the top surface of the tray.
  • the retainer lid 56 is secured to the distal end 64 of the tray 54 via the snap-fit projections and snap-fit depressions.
  • the four snap-fit projections 138A-138D projecting from the bottom surface of the retainer lid 56 are inserted into the four snap-fit depressions 104A-104D formed in the top surface of the tray 54.
  • the first snap-fit projection 134A on the retainer lid 56 desirably passes through the elongated cutout 158 on the top panel 140 and the second cutout 168 on the connecting panel 164 for attaching the retainer sleeve 58 to the tray 54.
  • the fourth snap-fit projection 134D on the retainer lid 56 passes through the elongated slot 158 on the top panel 140 and into the fourth snap-fit depression on the tray 54 for attaching the retainer sleeve 58 to the tray.
  • the retainer lid 56 may be split into two smaller retainer lids instead of one larger retainer lid to minimize material costs.
  • the two smaller retainer lids desirably perform the same functions as the single retainer lid 56 shown and described herein.
  • the distal end of the retainer lid may be secured to the distal end of the tray via a hinge element.
  • the connected retainer lid may be pivoted about the hinge element from a first position to a second position for opposing and covering the top surface of the tray at the distal end of the tray.
  • the top panel 140 desirably overlies the top surface of the tray at the proximal end 62 of the tray with the proximal edge 150 of the top panel 140 being substantially aligned with the proximal end 62 of the tray 54.
  • the bottom panel 142 desirably extends over the bottom surface 74 of the tray.
  • the top panel 140 of the retainer sleeve 58 overlies the top surface of the tray 54.
  • the top panel 140 desirably conforms to the sloping top surface of the tray 152 and slopes downwardly between the proximal end 62 and distal end 64 of the tray.
  • the handle 55 of the medical device 52 lies adjacent the first and second retaining posts 101, 102 for preventing the medical device 52 from sliding in a proximal direction toward the proximal end 62 of the tray 54.
  • the retainer sleeve 58 is wrapped around the proximal end 62 of the tray 54 with the top panel 140 overlying the handle 53 of the medical device 52 and the top surface of the tray 54.
  • the cutout 156 formed the top panel 140 of the retainer sleeve 58 desirably enables the top panel 140 to be flexed away from the top surface of the tray in the direction indicated R 1 .
  • the retainer sleeve 58 is “closed” along the second lateral side 68 of the tray 54, and is “open” along the proximal end 62 and the first lateral side 66 of the tray 54.
  • the "closed” portion of the retainer sleeve 58 prevents the medical device 52 from being removed via the second lateral side 68 of the tray, however, the "open” portions of the retainer sleeve 58 enable the top panel 140 to be flexed away from the top surface 72 of the tray 54 so that the medical device may be pivoted away from the tray (see FIG. 9F for movement designated R 1 ), whereby the handle 53 clears the retainer posts 100, 102. Once the handle clears the retainer posts, the handle 53 may be pulled proximally through the "opening" at the proximal end of the retainer sleeve 58 at the proximal end 62 of the tray 54.
  • the assembled package 50 containing the medical device 52 is inserted through an open end of a sealable outer pouch 60.
  • the outer pouch is preferably sealed along a first lateral edge 170, a proximal edge 172 and a second lateral edge 174.
  • the distal edge 176 is open for receiving the package.
  • the proximal end 62 of the tray 54 is inserted into the open end 176 of the pouch 60 in the direction indicated A 1 .
  • the thicker proximal section 62 of the tray 54 is the first end of the tray to be inserted into the pouch and is trailed by the thinner, distal end 64 of the tray.
  • the outer pouch is preferably a sealable foil pouch including first and second foil sheets that are joined together as disclosed in commonly assigned U.S. Patent No. 8,292,076 to Dacey.
  • FIG. 9H shows the package 50 after it has been further inserted into the outer pouch 60.
  • FIG. 9I shows the outer pouch 60 after the package 50 has been fully inserted therein.
  • EtO gasses are circulated throughout the interior of the pouch 60 and around the medical device and the tray and, after vacuum drying, the open end 176 of the outer pouch is sealed for completely sealing the outer pouch.
  • the outer pouch 60 includes an opening tab 178 that is provided in a corner of the pouch located between the proximal edge 172 and the second lateral edge 174. Referring to FIGS.
  • the openings in the retainer sleeve 58 located along the first lateral side 66 and the proximal end 62 of the tray 54 are preferably disposed adjacent the opening tab 178 of the outer pouch 60 to provide for easy access to the handle of the medical device when the opening tab 178 is peeled open.
  • the assembled package including the medical device and the outer pouch are subjected to a sterilization process to sterilize the medical device and the components of the package.
  • a sterilization process may involve a gas diffusion sterilization method.
  • the sterilization method preferably involves using ethylene oxide (EtO) gasses.
  • Ethylene oxide is commonly used in the healthcare industry for sterilizing medical devices because of its non-damaging effects on delicate instruments and devices that must be sterile, and for its compatibility with a wide range of packaging materials.
  • EtO methods are frequently used for medical devices having parts that cannot tolerate heat, moisture or abrasive chemicals, such paper, rubber and plastic parts. Using EtO gasses for the sterilization of medical devices was initially developed by the U.S. military and remains the most commonly used in many industries.
  • the open end 176 of the pouch 60 is sealed so that the package is fully sealed within the outer pouch 60.
  • the surgical personnel may reach into the opened pouch 60 to access the medical device 52 disposed on the tray 54.
  • a surgeon places his or her hand between the top panel 140 of the retainer sleeve 58 and the central depression 180 located between the first and second retainer posts 100, 102 to grasp the handle 53 of the medical device 52 with the thumb, fingers and palm of the hand.
  • the handle 53 is preferably pivoted about its base in the direction R 1 so that the handle 53 is clear of the first and second retaining elements 100, 102.
  • the cut 156 formed in the top panel 140 enables the top panel 140 to flex away from the top surface 72 of the tray 54.
  • the retainer lid 56 secures the distal end 152 of the retainer sleeve 58 to the top surface of the tray.
  • the medical device 52 may be pulled in a proximal direction relative to the tray 54 for removing the medical device 52 from the tray.
  • a package 250 for a medical device 252 preferably includes a tray 254 adapted to receive the medical device 252, and a retainer lid 256 that is adapted to be secured to the tray 254, such as being snap-fit onto a distal end of the tray 254.
  • the package desirably includes a retainer sleeve 258 that is wrapped around a proximal end of the tray 254 and is secured to the tray via the retainer lid 256.
  • the assembled package may be inserted into an open end of a sealable, outer pouch 260 for being sterilized and sealed (e.g., air-tight sealed) within the outer pouch.
  • the tray 254 desirably includes a proximal end 262, a distal end 264, a first lateral side 266, and a second lateral side 268.
  • the tray 254 preferably has a flange 270 that extends around the outer perimeter of the tray. Referring to FIG. 12C , the flange 270 preferably divides the tray 254 between a top surface 272 configured to receive a medical device, and a bottom surface 274 that is opposite the top surface 272.
  • the tray 254 is preferably a thermoformed tray that includes a first channel 276 defining a depression molded in the top surface of the tray that is adapted to receive a handle of the medical device 252 ( FIG. 11 ).
  • the tray 254 also desirably includes an elongated second channel 278 molded therein that is adapted to receive the elongated shaft of the medical device 252 ( FIG. 11 ).
  • the first channel 276 desirably includes a centrally located depression 280 bounded on one side by a first flat surface 282 and a second side by a second flat surface 284.
  • the distal end of the central depression 280 desirably includes a concave-shaped cutout 288 formed in a mound 290 of the tray 254 that is located between the first channel 276 and the second channel 278.
  • the mound 290 preferably includes a proximal flat section 292 and a distal sloping section 294 that slopes downwardly toward the bottom surface 274 of the tray 254. As shown in FIG. 12C , the distal sloping section 294 of the mound 290 slopes downwardly toward the distal end 264 and the bottom surface 274 of the tray 254. Referring to FIG. 12C , in one embodiment, the proximal end 262 of the tray is thicker than the distal end 264 of the tray 254.
  • the second channel 278 desirably includes a first wall 296 and an opposing second wall 298.
  • the first and second walls 296, 298 are generally straight and conform to the shape of the elongated shaft of the medical device 252 ( FIG. 11 ).
  • the tray 254 desirably includes a pair of spaced retention posts 300, 302 that are located adjacent the proximal end 262 of the tray.
  • the proximally located retention posts 300, 302 are desirably spaced from one another by the central depression 280 formed in the top surface of the tray.
  • the retention posts 300, 302 retain the medical device on the tray 254 and prevent the medical device from sliding and/or moving (e.g., proximally) relative to the tray. In one embodiment, the medical device will not fall out of the tray 254 and will be retained inside the tray by the retention posts 300, 302 and the proximal face of the mound 290.
  • the medical device may be removed from the tray by rotating the handle away from the top surface of the tray until the handle is clear of the retention posts 300, 302. Once the handle is clear of the retention posts 300, 302, the medical device may be pulled toward the proximal end 262 of the tray 254 for removing the medical device from the tray.
  • the distal end 264 of the tray 254 desirably includes four snap-fit depression 304A-304D that are adapted to receive similarly shaped snap-fit projections extending from an underside of the retainer lid 256 ( FIG. 11 ), as will be described in more detail herein.
  • the tray 254 preferably includes a first pair of EtO gas circulation chambers 306A, 306B for circulating EtO gasses that are located between the first and second snap-fit depressions 304A, 304B, the outer perimeter flange 270 extending along the first lateral side 266 of the tray, and the first wall 296 of the second channel 278.
  • the top surface of the tray 254 also desirably includes a second pair of EtO gas circulating chambers 308A, 308B that are located between the third and fourth snap-fit depressions 304C, 304D, the outer perimeter flange 270 extending along the second lateral side 268 of the flange, and the second wall 298 of the second channel 278.
  • the top surface of the tray 254 desirably includes a number of EtO gas circulating grooves formed therein to ensure that the EtO gasses may easily circulate throughout the tray.
  • the tray includes a first groove 310 that provides fluid communication between the first snap-fit depression 304A and the chamber 306A, a second groove 312 that provides fluid communication between the chamber 306A and the second channel 278, and a third groove 314 that provides fluid communication between the second snap-fit depression 104B and the chamber 306B.
  • the top surface of the tray 254 also desirably includes a fourth groove 316 that provides fluid communication between the chamber 306B and the second channel 278, a fifth groove 318 that provides fluid communication between the third snap-fit depression 304C and the chamber 308B, and a sixth groove 320 that provides fluid communication between the chamber 308B and the second channel 278.
  • the tray 254 preferably includes a seventh groove 322 that provides fluid communication between the fourth snap-fit depression 304D and the chamber 308A, and an eighth groove 324 that provides fluid communication between the chamber 308A and the second channel 278.
  • the EtO gasses preferably pass over the top and bottom surfaces of the tray and through the first channel 276 and second channel 278.
  • the EtO gasses also preferably pass through the grooves 310-324 and into the chambers 306A, 306B, 308A, and 308B and the four snap-fit depressions 304A-304D for circulating the sterilization gasses throughout the tray 254.
  • the tray 254 has a length L 5 of about 30,48-40,64 cm (12-16 inches) and more preferably about 37,78 cm (14.875 inches). and a width W 5 of about 15,24- 20,32 cm ( 6-8 inches) and more preferably 19,32 cm (7.606 inches).
  • the tray 254 preferably includes spacers 322A-322F projecting from the bottom of the peripheral flange 270.
  • three spacers 325A-325C extend along the first lateral side 266 of the tray
  • a single spacer 325D extends along the distal end 264 of the tray
  • three spacers 325F-325G extend along a second lateral side 268 of the tray
  • a single spacer 325H extends along a proximal end 262 of the tray.
  • Other embodiments may have more or fewer spacers on the flange. As shown in FIGS.
  • the spacers 325 preferably project from the bottom surface 274 of the flange 270 to space the flange 270 away from an opposing inner surface of the outer pouch 260 ( FIG. 11 ). Spacing the flange 270 away from the opposing inner surface of the pouch ensures thorough and efficient circulation of the EtO gasses and also ensures that the outer flange 270 will not damage (e.g., cut) an opposing seal formed inside the outer pouch 260.
  • the retention posts 300, 302 and the eighth spacer 325H define a height H 4 of about 2,54- 5,08 cm (1-2 inches) and more preferably about 3,78 cm (1.490 inches).
  • the tray 254 preferably narrows and becomes thinner between the proximal end 262 and the distal end 264. In other words, the tray 254 tapers inwardly between the proximal end 262 and the distal end 264 so that the distal end 264 of the tray is thinner than the proximal end 262 of the tray.
  • the spacers 325 preferably define a height H 5 between the flange 270 and the lower end of the spacer of about 0,254- 0,508 cm ( 0.10-0.20 inches ) and more preferably about 0,396 cm (0.156 inches).
  • the retainer lid 256 ( FIG. 11 ) desirably has a length L 6 of about 50,8- 63,5 cm (20-25 inches) and more preferably about 60,45 cm (23.8 inches) and a width W 6 of about 20,32- 30,48 cm (8-12 inches) and more preferably about 26,26 cm (10.34 inches).
  • the retainer lid 256 is preferably snap-fit onto the distal end of the tray 254 ( FIGS. 12A-12D ) for securing a distal end of a medical device in the tray and for securing a retainer sleeve onto the tray.
  • the underside of the retainer lid has molded projections 355A, 355B that engage the shaft to prevent lateral shifting of the medical device in the second channel 278 of the tray 254 ( FIG. 12B ).
  • the retainer lid 256 ( FIG. 11 ) preferably includes a top surface 330 and a bottom surface 332.
  • the retainer lid is made of polypropylene (PP).
  • the retainer lid 256 desirably includes four snap-fit protrusions 334A-334D that project from the bottom surface 332.
  • the retainer lid 256 desirably includes a first pair of depressions 336A, 336B that conform in size and shape to the first pair of chamber 306A, 306B on the tray 254 ( FIGS.
  • each snap-fit projection 334A-334D preferably defines a height H 6 of about 0,762- 0,889 cm ( 0.300-0.350 inches) and more preferably about 0,813 cm (0.320 inches).
  • the retainer sleeve 258 ( FIG. 11 ) preferably includes a foldable blank, such as a paperboard blank, having a top panel 340, a bottom panel 342 and a connecting panel 344.
  • a first fold line 346 desirably extends between the top panel 340 and the bottom panel 342 for facilitating folding of the top panel and the bottom panel relative to one another.
  • the retainer sleeve 258 desirably includes a second fold line 348 that extends between the bottom panel 342 and the connecting panel 344 for facilitating folding of the bottom panel and the connecting panel relative to one another.
  • the top panel 340 desirably includes a proximal edge 350, a distal edge 352 and an outer edge 354.
  • the top panel 340 desirably includes a cut 356 formed therein that extends from the outer edge 354 toward the first fold line 346.
  • the cut 356 has a length L 3 of about 3,81- 4,45 cm (1.50-1.75 inches) and more preferably about 4,29 cm (1.69 inches).
  • the top panel 340 includes an elongated cutout 358 that extends along the distal edge 352 thereof.
  • the elongated cutout 358 has a length L 4 of about 11,43- 12,70 cm (4.50-5.00 inches) and more preferably about 12,22 cm (4.81 inches) and a width W 3 of about 1,27- 2,54 cm ( 0.50-1.00 inches) and more preferably about 2,21 cm (0.87 inches).
  • a first pair of notches 360A, 360B may be provided at the ends of the first fold line 346 for facilitating folding of the top panel 340 and the bottom panel 342 relative to one another.
  • the retainer sleeve 258 may also include a second pair of notches 362A, 362B provided at the ends of the second fold line 348 for facilitating folding of the bottom panel 342 and the connecting panel 344 relative to one another.
  • the connecting panel 344 desirably includes a proximal edge 364 and a distal edge 366.
  • the connecting panel preferably has a second cutout 368 formed adjacent the distal edge 366 thereof.
  • the retainer sleeve 258 is folded for being wrapped about the tray 254 ( FIGS. 12A-12D ).
  • the connecting panel 364 is preferably folded over the bottom panel 342 and the top panel 340 is folded over the connecting panel 364.
  • the elongated cutout 358 on the top panel 340 is preferably aligned with the second cutout 368 on the connecting panel 364.
  • the first snap-fit projection 334A on the retainer lid ( FIG. 13A ) is passed through the aligned elongated cutout 358 and the second cutout 368 for securing the distal end of the retainer sleeve 258 to the tray 254 ( FIG. 12A ).
  • the medical device 252 is disposed on the tray 254 so that the handle 252 is in the first channel 276 and the elongated shaft 265 is in the second channel 278.
  • the bottom surface of the tray is desirably positioned over the bottom panel 342 of the retainer sleeve 258.
  • the connecting panel 344 of the retainer sleeve 258 is folded over the second lateral edge 268 of the tray 254 so that the second cutout 368 on the connecting panel 344 overlies the fourth snap-fit depression 304D on the tray 254.
  • the top panel 340 of the retainer sleeve 258 is folded over the top surface of the tray so that the elongated cutout 358 is aligned with the first snap-fit depression 304A and the fourth snap-fit depression 304D on the tray 254.
  • the top panel 340 preferably overlies the connecting panel 344 with the elongated cutout 358 overlying the second cutout 368, which, in turn, is aligned with the fourth snap-fit depression 304D.
  • the retainer lid 256 is preferably secured to the distal end of the top surface of the tray 254 with the four snap-fit projections 334A-334D ( FIG. 13C ) on the retainer lid 256 inserted into the corresponding four snap-fit depressions 304A-304D formed on the tray 254.
  • the first snap-fit projection 334A on the retainer lid passes though the elongated slot 358 and into the first snap-fit depression 304A on the tray.
  • the fourth snap-fit projection 334D of the retainer lid 256 passes through the elongated cutout 358 of the top panel 340, the second cutout 368 of the connecting panel 344, and is secured by the fourth snap-fit depression 304D for securing the retainer sleeve 258 over the proximal end of the tray 254.
  • the top panel 340 of the retainer sleeve 258 overlies the top surface of the tray at the proximal end 262 of the tray 254.
  • the cut 356 provided in the top panel 340 enables a free edge of the top panel 340 to flex away from the top surface of the tray 254 for accessing the medical device stored on the tray.
  • the retainer sleeve 358 wraps around the tray so that the bottom panel 342 of the retainer sleeve overlies the bottom surface 274 of the tray 254.
  • the proximal end 362 of the tray 254 of the package 250 is inserted into an open end 376 of the outer pouch 260.
  • FIG. 16F shows the tray 254 of the package 250 after it has been further inserted into open end 376 of the outer pouch 260.
  • FIG. 16G shows the outer pouch 260 after the multi-component package has been fully inserted therein.
  • the outer pouch 260 preferably includes a first sealed lateral edge 370, a sealed distal edge 372 and a second sealed lateral edge 374.
  • the outer pouch 260 also includes the open, unsealed proximal edge 376 that enables the interior of the pouch and the package loaded therein to be sterilized using EtO gasses that are circulated throughout the interior of the pouch 260 and around the tray and the medical device. Once the interior of the pouch and the package have been sterilized using EtO gasses, the open proximal end 376 may be sealed for completely sealing the package within the outer pouch 260.
  • a corner of the sealed pouch 260 desirably includes a corner opening tab 378 that may be peeled apart for opening the sealed pouch and accessing the medical device loaded onto the tray.
  • a package 450 for a medical device 452 preferably includes a tray 454 adapted to receive the medical device 452, a retainer lid 456 that is snap-fit onto a distal end of the tray 454, and a cover flap 458 that is attached to one lateral side of the tray 454 and that is secured to the top surface of the tray 454 by the retainer lid 456.
  • the assembled package 450 may be inserted into an open end of a sealable outer pouch, such as a foil pouch.
  • the tray 454 of the package desirably includes a proximal end 462, a distal end 464, a first lateral side 466, and a second lateral side 468.
  • the tray 454 preferably has a peripheral outer flange 470 that extends around the outer perimeter of the tray.
  • the cover flap 458 preferably includes a paperboard blank having a top panel 540 with a lateral edge 546 that is preferably attached to the second lateral side 468 of the tray for forming a closed side of the cover flap 458 that extends along the second lateral side 468 of the tray.
  • the cover flap 458 desirably includes a proximal edge 550, a distal edge 552, an outer edge 554, and the lateral edge 546.
  • the cover flap 458 desirably includes a cut 556 formed therein that extends from the outer edge 554 toward the lateral edge546.
  • the cover flap 458 preferably includes an elongated cutout 558 that extends along the distal edge 552 thereof.
  • the cover flap 458 desirably covers the top surface of the tray 454 at the proximal end of the tray.
  • the lateral edge 546 of the cover flap is preferably secured to the second lateral edge 468 of the tray 454 (e.g., by a securing element) to form a closed side of the cover flap.
  • One or more of the projections on the retainer lid 456 desirably pass through the elongated slot 558 on the cover flap 458 for securing the distal end 552 of the cover flap 458 to the top surface of the tray 454.
  • the cover flap 458 When secured to the tray 454, the cover flap 458 has a closed side that extends along the second lateral side 468 of the tray, a first open side that extends along the proximal edge 462 of the tray, and a second open side that extends along the first lateral edge 466 of the tray 454.
  • the cover flap 458 is preferably flexed away from the top surface of the tray for accessing the medical device 452. As the handle of the medical device is rotated away from the top surface of the tray, the first and second open sides of the cover flap 458 preferably move away from the top surface of the tray 454 to allow for removal of the medical device 452 from the tray, such as shown and described herein (e.g., in FIGS. 10A-10B ).

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Surgery (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Medical Informatics (AREA)
  • Molecular Biology (AREA)
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  • General Health & Medical Sciences (AREA)
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  • Packages (AREA)

Claims (15)

  1. Emballage (50) pour un dispositif médical (52), comprenant:
    un plateau (54) présentant une surface supérieure (72), une surface inférieure (74), une extrémité proximale (62), une extrémité distale (64), et des premier et second côtés latéraux (66, 68) qui s'étendent entre les extrémités proximale et distale (62, 64), ledit plateau (54) présentant des éléments faisant saillie à partir de ladite surface supérieure (72);
    un couvercle de retenue (56) fixé audit plateau (54) afin de couvrir ladite surface supérieure (72) dudit plateau (54) à l'extrémité distale (64) dudit plateau (54);
    caractérisé en ce que l'emballage comprend en outre soit:
    (i) un manchon de retenue (58) présentant une extrémité distale et une extrémité proximale, l'extrémité distale dudit manchon de retenue (58) étant enroulée autour desdites surfaces supérieure et inférieure (72, 74) dudit plateau (54) et étant fixée audit plateau (54) par ledit couvercle de retenue (56), l'extrémité proximale dudit manchon de retenue (58) comprenant un panneau supérieur qui couvre ladite surface supérieure (72) dudit plateau (54) à l'extrémité proximale (62) dudit plateau (54), dans lequel ledit panneau supérieur dudit manchon de retenue (58) présente un bord libre qui est adapté pour se fléchir à l'écart de ladite surface supérieure dudit plateau (54); soit
    (ii) un volet de recouvrement (458) présentant une extrémité proximale, une extrémité distale, et un côté latéral qui s'étend entre les extrémités proximale et distale, le côté latéral du volet de recouvrement étant fixé à l'un des côtés latéraux dudit plateau (54) et l'extrémité distale dudit volet de recouvrement étant fixée audit plateau (54) par ledit couvercle de retenue (56), dans lequel ledit volet de recouvrement couvre ladite surface supérieure (72) dudit plateau (54) à l'extrémité proximale (62) dudit plateau (54), dans lequel ledit volet de recouvrement présente un bord libre qui est adapté pour se fléchir à l'écart de ladite surface supérieure (72) dudit plateau (54).
  2. Emballage (50) selon la revendication 1, dans lequel ledit emballage comprend ledit manchon de retenue (58), dans lequel ledit manchon de retenue (58) comporte une encoche qui s'étend entre ledit bord libre dudit panneau supérieur et l'extrémité distale dudit manchon de retenue (58) afin de permettre audit bord libre dudit panneau supérieur de se déplacer par rapport à l'extrémité distale dudit manchon de retenue (58) .
  3. Emballage (50) selon la revendication 1, dans lequel lesdits éléments faisant saillie à partir de ladite surface supérieure dudit plateau (54) sont des éléments moulés qui définissent un premier canal à proximité de l'extrémité proximale dudit plateau (54), un second canal distant dudit premier canal qui s'étend en direction de l'extrémité distale dudit plateau (54), et au moins un élément de retenue situé à l'extrémité proximale dudit plateau (54); ou, optionnellement additionnellement,
    dans lequel ledit au moins un élément de retenue comprend une paire de montants de retenue qui sont espacés l'un de l'autre à l'extrémité proximale dudit plateau (54); ou, optionnellement additionnellement,
    dans lequel lesdits éléments moulés comprennent en outre un renflement situé entre lesdits premier et second canaux, dans lequel ledit renflement présente une surface supérieure comprenant une section proximale plate et une section distale inclinée qui est inclinée vers le bas en direction de l'extrémité distale dudit plateau (54); ou, optionnellement additionnellement,
    dans lequel lesdits premier et second canaux se coupent mutuellement au niveau dudit renflement; ou, optionnellement additionnellement,
    dans lequel lesdits premier et second canaux définissent des évidements moulés dans ledit plateau (54) et ledit renflement fait saillie au-dessus desdits premier et second canaux; ou, optionnellement additionnellement,
    dans lequel ledit renflement présente une face proximale qui est opposée auxdits premier et second montants de retenue; ou, optionnellement additionnellement,
    dans lequel ladite surface supérieure dudit plateau (54) comprend en outre une dépression centrale qui s'étend entre le bord proximal et ladite face proximale dudit renflement, et dans lequel ladite dépression centrale est située entre lesdits premier et second montants de retenue.
  4. Emballage (50) selon la revendication 3, comprenant en outre un dispositif médical (52) présentant une poignée et un arbre allongé qui s'étend à partir de ladite poignée, dans lequel ladite poignée est disposée dans ledit premier canal dudit plateau (54) et ledit arbre allongé est disposé dans ledit second canal dudit plateau (54).
  5. Emballage (50) selon la revendication 4, dans lequel ledit emballage comprend ledit manchon de retenue (58), dans lequel ledit panneau supérieur dudit manchon de retenue (58) couvre ladite poignée dudit dispositif médical (52), et dans lequel ledit manchon de retenue (58) comporte une encoche qui s'étend entre ledit bord libre dudit panneau supérieur et l'extrémité distale dudit manchon de retenue (58), dans lequel ladite encoche dudit manchon de retenue (58) permet audit bord libre dudit panneau supérieur d'être fléchi à l'écart de ladite poignée et de ladite surface supérieure dudit plateau (54) de manière à permettre un enlèvement dudit dispositif médical (52) dudit plateau (54) .
  6. Emballage (50) selon la revendication 4, dans lequel ladite surface supérieure dudit plateau (54) présente une ou plusieurs dépression (s) d'encliquetage moulée(s) dans celle-ci à l'extrémité distale dudit plateau (54), et ledit couvercle de retenue (56) comporte une ou plusieurs saillie(s) d'encliquetage moulée(s) dans celui-ci qui s'étendent à partir d'une surface inférieure de celui-ci, et dans lequel ladite/lesdites une ou plusieurs saillie(s) d'encliquetage dudit couvercle de retenue (56) est (sont) insérable(s) dans ladite/lesdites une ou plusieurs dépression(s) d'encliquetage dudit plateau (54) afin de fixer ledit couvercle de retenue (56) audit plateau (54).
  7. Emballage (50) selon la revendication 5, dans lequel l'extrémité distale dudit manchon de retenue (58) comporte une ou plusieurs entaille(s) qui sont alignées avec au moins une de ladite/desdites une ou plusieurs dépression(s) d'encliquetage moulée(s) dans ledit plateau (54), et dans lequel au moins une de ladite/desdites une ou plusieurs saillie(s) d'encliquetage sur ledit couvercle de retenue (56) passe(nt) à travers ladite/lesdites une ou plusieurs entaille(s) pour fixer l'extrémité distale dudit manchon de retenue (58) audit plateau (54).
  8. Emballage (50) selon la revendication 6, dans lequel ledit emballage comprend ledit manchon de retenue (58), dans lequel ledit manchon de retenue (58) comprend:
    un panneau inférieur qui couvre ladite surface inférieure dudit plateau (54);
    ledit panneau supérieur attaché à un premier bord dudit panneau inférieur; et
    un panneau de connexion attaché à un second bord dudit panneau inférieur, dans lequel ledit manchon de retenue (58) enroulé autour dudit plateau (54) couvre lesdits premier et second côtés latéraux dudit plateau (54) .
  9. Emballage (50) selon la revendication 1, dans lequel ledit plateau (54) comprend du polyéthylène à haute densité (HDPE), ledit couvercle de retenue (56) comprend du polypropylène (PP) et ledit manchon de retenue (58) ou volet de recouvrement (458) comprend du carton.
  10. Emballage selon la revendication 1, dans lequel ledit plateau (54) est plus épais à l'extrémité proximale et plus mince à l'extrémité distale.
  11. Emballage (50) selon la revendication 1, comprenant en outre une poche extérieure (60) adaptée pour recevoir ledit plateau (54), ledit couvercle de retenue (56) et ledit manchon de retenue (58) ou volet de recouvrement (458), dans lequel ladite poche extérieure (60) est fermable pour former un joint étanche à l'air.
  12. Emballage (50) selon la revendication 1, dans lequel ledit plateau (54) comprend une bride périphérique qui s'étend autour du périmètre extérieur dudit plateau (54), et dans lequel ladite surface supérieure dudit plateau (54) est située au-dessus de ladite bride périphérique et ladite surface inférieure dudit plateau (54) est située en dessous de ladite bride périphérique.
  13. Emballage (50) pour un dispositif médical (52), selon la revendication 1, comprenant:
    un plateau thermoformé; un dispositif médical (52) disposé sur ladite surface supérieure dudit plateau, ledit dispositif médical (52) comprenant une poignée et un arbre allongé qui fait saillie à partir de ladite poignée;
    ledit plateau comprenant un premier canal pour recevoir ladite poignée, un second canal pour recevoir ledit arbre allongé, un renflement situé entre lesdits premier et second canaux, et une paire de montants de retenue situés à l'extrémité proximale dudit plateau, dans lequel ladite poignée est disposée entre lesdits montants de retenue et ledit renflement afin de minimiser le déplacement proximal et distal dudit dispositif médical (52) par rapport audit plateau;
    un couvercle de retenue thermoformé fixé audit plateau pour couvrir ledit arbre allongé dudit dispositif médical (52) à l'extrémité distale dudit plateau;
    un manchon de retenue (58) couvrant lesdites surfaces supérieure et inférieure dudit plateau, avec l'extrémité distale dudit manchon de retenue (58) qui est fixée audit plateau par ledit couvercle de retenue, et le manchon de retenue (58) pouvant offrir un accès à ladite poignée dudit dispositif médical (52), dans lequel ladite poignée présente une base et ladite poignée peut pivoter autour de ladite base afin de dégager ladite poignée desdits montants de retenue de telle sorte que ledit dispositif médical (52) soit déplaçable dans une direction proximale pour enlever ledit dispositif médical (52) dudit plateau.
  14. Emballage (50) selon la revendication 13, dans lequel ledit plateau thermoformé comprend du polyéthylène à haute densité (HDPE), ledit couvercle de retenue thermoformé comprend du polypropylène (PP), et ledit manchon de retenue (58) comprend du carton.
  15. Emballage (50) selon la revendication 13, dans lequel lesdits éléments faisant saillie à partir de ladite surface supérieure dudit plateau (54) sont des éléments moulés.
EP14795923.3A 2013-11-04 2014-10-27 Emballages à éléments multiples pour dispositifs médicaux Active EP3065665B1 (fr)

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US14/071,310 US9265578B2 (en) 2013-11-04 2013-11-04 Multi-component packages for medical devices
PCT/US2014/062412 WO2015065903A1 (fr) 2013-11-04 2014-10-27 Emballages à éléments multiples pour dispositifs médicaux

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Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2506370B (en) * 2012-09-26 2014-10-15 Medicart Int Ltd Vacuum storage system
CA2880380C (fr) * 2012-09-28 2020-09-15 Sofradim Production Emballage pour dispositif de reparation des hernies
WO2017023338A1 (fr) * 2015-08-06 2017-02-09 Jacobs Emerging Technologies, Llc Support de dispositif médical
US10485627B2 (en) * 2016-04-07 2019-11-26 Ethicon, Inc. Containment sleeves for packages containing medical devices
US20170354474A1 (en) * 2016-06-09 2017-12-14 Amt Group Bahamas Ltd. Tee probe container
US10897062B2 (en) 2016-06-13 2021-01-19 Nec Corporation Lithium ion secondary battery
US10470835B2 (en) * 2017-01-25 2019-11-12 DePuy Synthes Products, Inc. Single use disposable sterile kit
CN107031985B (zh) * 2017-06-03 2020-02-18 王海涛 一种用于医疗器械的组合包装系统
US10577165B2 (en) 2017-09-25 2020-03-03 SEE Forming L.L.C. Key retention system for product packaging
US20190184221A1 (en) * 2017-12-18 2019-06-20 Depco, Inc. Tray for holding exercise putty and putty tools
CN108216929B (zh) * 2017-12-29 2019-06-18 江苏风和医疗器材股份有限公司 包装盒
USD848845S1 (en) * 2018-03-23 2019-05-21 Ethicon, Inc. Packaging tray for a medical device
US11155381B1 (en) 2018-10-08 2021-10-26 SEE Forming L.L.C. Joinable thermoform product packaging
WO2020077161A1 (fr) 2018-10-11 2020-04-16 Freeflow Medical Devices Llc Emballage pour dispositifs médicaux revêtus de liquides perfluorés ou de dispersions de ceux-ci
CN109363778B (zh) * 2018-12-20 2021-04-20 鹤壁市人民医院 一种便携式的多功能心脏内科检测仪
AU2019416199A1 (en) 2018-12-26 2021-05-27 Boston Scientific Scimed, Inc. Medical device containment and transportation systems and methods
US11432817B2 (en) * 2018-12-28 2022-09-06 Cilag Gmbh International Packaging for surgical stapler buttress
US11751986B2 (en) * 2019-01-04 2023-09-12 Cook Medical Technologies Llc Packaging system for ureteral stent
CA3165838A1 (fr) 2019-12-24 2021-07-01 Boston Scientific Scimed, Inc. Systemes de transport de dispositif medical
US11696811B2 (en) 2019-12-24 2023-07-11 Boston Scientific Scimed, Inc. Medical device transportation systems
WO2021157668A1 (fr) 2020-02-07 2021-08-12 国立研究開発法人物質・材料研究機構 Composé polymère, procédé de production d'un composé polymère, composition adhésive, produit durci, procédé de production de composition adhésive, et procédé d'ajustement de la force adhésive
CN113387032A (zh) * 2021-06-10 2021-09-14 泰州健朗医疗器械有限公司 胸腹腔穿刺引流系统包装装置

Family Cites Families (73)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3724651A (en) 1971-03-03 1973-04-03 Johnson & Johnson Peelable surgical package
US3926309A (en) 1973-08-01 1975-12-16 Vicra Sterile Inc Two layer sterile packaging
US3985289A (en) * 1975-04-10 1976-10-12 Eli Lilly And Company Two-piece container
US4206844A (en) 1977-01-04 1980-06-10 Toppan Printing Co., Ltd. Package for a sterilized material
US4332322A (en) 1980-09-02 1982-06-01 Champion International Corporation Folder to hold coil of plastic tubing with clamp and fittings
US4511035A (en) 1983-01-13 1985-04-16 Ethicon, Inc. Package for surgical instrument
USD282684S (en) 1983-06-10 1986-02-18 Aspen Laboratories, Inc. Electrosurgical pencil holster
USD282482S (en) 1983-07-29 1986-02-04 A - L - S Mfg. Co. Inc. Holster for capsule-implanting gun or the like
FR2602752B1 (fr) 1986-08-12 1988-11-10 Oreal Ensemble pour le conditionnement separe d'au moins deux produits ne devant etre mis en contact qu'au moment de l'emploi et pour la realisation de cette mise en contact
US5165540A (en) * 1990-01-10 1992-11-24 Sherwood Medical Company Angiographic catheter package
IE62145B1 (en) 1990-01-30 1994-12-14 Bard C R Ireland Ltd Catheter packaging system
US5031775A (en) 1990-02-14 1991-07-16 Angeion Corporation Medical instrument holder
ATE118188T1 (de) 1990-04-04 1995-02-15 American National Can Co Kontrollierbare, leicht zu öffnende verpackung.
US5098391A (en) 1990-04-09 1992-03-24 Abbott Laboratories Dispensing system for pacing lead
US5106662A (en) 1990-10-15 1992-04-21 Kamil Khayat Flower wrapper
US5226535A (en) 1992-02-14 1993-07-13 Ethicon, Inc. Package for endoscopic suture loop and cannula
US5234106A (en) 1992-06-11 1993-08-10 Ethicon, Inc. Package retainer for sterile instruments
US5284244A (en) * 1992-08-31 1994-02-08 Ethicon, Inc. Sterile package for surgical instruments
US5318543A (en) * 1992-10-08 1994-06-07 Abbott Laboratories Laparoscopic jejunostomy instrumentation kit
US5351822A (en) 1993-02-17 1994-10-04 United States Surgical Corporation Retainer for an elongated surgical instrument
EP0613697B1 (fr) 1993-02-17 1996-07-17 Schneider (Europe) Ag Emballage pour un instrument médical allongé
US5353929A (en) 1993-04-19 1994-10-11 United States Surgical Corporation Package for surgical instrument
US5447230A (en) * 1993-07-23 1995-09-05 Ethicon, Inc. Package for surgical instruments
USD356677S (en) 1993-08-13 1995-03-28 K & W Enterprises, Inc. Gun holster
US5375717A (en) 1993-08-31 1994-12-27 Ethicon, Inc. Foldable package for endoscopic components and the like
US5487469A (en) 1994-01-26 1996-01-30 Ethicon, Inc. Package for endoscopic instrument
NL9400214A (nl) 1994-02-10 1995-09-01 Cordis Europ Catheterverpakking.
US5497601A (en) 1994-08-19 1996-03-12 Cordis Corporation Packaging having discrete retainers for a medical catheter and method
US5498242A (en) 1995-04-24 1996-03-12 Cooke; Thomas H. Medical needle sheath and stand for one-handed use
US5655657A (en) 1995-09-25 1997-08-12 Ethicon, Inc. Package for specimen retrieval bag
EP0800789A1 (fr) 1996-04-10 1997-10-15 Ethicon, Inc. Emballage pour dispositif d'ancrage de suture
US5601189A (en) 1996-05-17 1997-02-11 Ethicon, Inc. Folder package for electrosurgical scissors
USD395359S (en) 1996-08-02 1998-06-23 Jan Reidar Olsen Bolt holster
US5699909A (en) 1996-08-07 1997-12-23 United States Surgical Corporation Surgical instrument package
AU132677S (en) 1997-06-13 1998-01-13 Hand saw holster
US5842567A (en) 1997-11-12 1998-12-01 Alcon Laboratories, Inc. Quick release package
US5888565A (en) * 1997-11-24 1999-03-30 Gics & Vermee, L.P. Food package including a tray with cover member having a raised top surface
US6047826A (en) 1998-03-18 2000-04-11 Ethicon, Inc. Package tray for meniscal needle
US5972008A (en) 1998-04-29 1999-10-26 Kalinski; Robert J. Method and apparatus for retaining a surgical mesh
US6261616B1 (en) * 1999-08-05 2001-07-17 Bordon Foods Corporation Microwavable meal kit and food packaging system
US6308875B1 (en) 1999-08-11 2001-10-30 Kristi M. Almo Surgical instrument storage pack
JP2001171738A (ja) * 1999-12-16 2001-06-26 Toyo Seikan Kaisha Ltd トレー容器用外装パッケージ
JP4505943B2 (ja) * 2000-05-09 2010-07-21 株式会社柏木モールド 包装容器
US6425900B1 (en) 2000-10-19 2002-07-30 Ethicon Endo-Surgery Method for attaching hernia mesh
US20020165549A1 (en) 2001-04-30 2002-11-07 Medtronic, Inc. Surgical instrument and attachment
US6986730B1 (en) 2001-08-17 2006-01-17 Todd Hoekstra Continuous web of breather pouches and automated method of packaging medical devices utilizing such pouches
US6994213B2 (en) 2001-09-18 2006-02-07 Becton, Dickinson And Company Packaging for push button blood collection set
FR2832052B1 (fr) * 2001-11-15 2004-10-29 Sofradim Production Dispositif d'emballage et de pliage d'une piece en materiau souple, notamment d'un renfort parietal
US6814236B2 (en) * 2001-12-31 2004-11-09 Ethicon, Inc. Blister tray with a package for a small device
FR2836816B1 (fr) 2002-03-08 2005-01-28 Sofradim Production Appareil de stockage, de distribution et de pose d'attaches chirurgicales en"i"couche
US6889839B1 (en) * 2002-05-07 2005-05-10 Perfecseal, Inc. Suspension package
US7247329B2 (en) 2003-01-31 2007-07-24 Kraft Foods Holdings, Inc. Double sealed pizza package and method of making
US7617932B2 (en) * 2003-09-19 2009-11-17 Diabetes Diagnostics, Inc. Medical device package, kit and associated methods
US20050092636A1 (en) 2003-10-31 2005-05-05 Wu Su-Syin Sterilization packaging
US20050189252A1 (en) 2004-02-19 2005-09-01 Naylor Jennifer R. Sterilization container
USD560490S1 (en) 2004-04-30 2008-01-29 General Mills Marketing, Inc. Packaging for dough product
US7281630B2 (en) * 2004-09-17 2007-10-16 Nokia Corporation Packaging
USD562549S1 (en) 2005-05-17 2008-02-26 Jeffrey David Bodnar Survival rifle holster
USD541933S1 (en) 2005-09-09 2007-05-01 Patient Shield Concepts, Llc Medical/dental suction nozzle holster
US7255230B1 (en) * 2006-06-16 2007-08-14 Paul Appelbaum Card and blister package
USD542525S1 (en) 2006-07-15 2007-05-15 Pacific Handy Cutter, Inc. Holster for safety cutter
CN104814768B (zh) 2006-09-12 2018-04-13 维达保健有限责任公司 医疗程序托盘及相关方法
USD576275S1 (en) 2006-11-06 2008-09-02 Patient Shield Concepts, Llc Medical/dental suction nozzle holster having notches
USD578642S1 (en) 2008-02-08 2008-10-14 Patient Shield Concepts, Llc Medical/dental suction nozzle holster having a universally adjustable strap
US8870049B2 (en) 2008-03-14 2014-10-28 Transenterix, Inc. Hernia stapler
CA2716820A1 (fr) 2008-03-14 2009-09-17 Safestitch Medical, Inc. Agrafeuse pour hernie avec manipulateur de filet integre
US8579920B2 (en) 2009-05-12 2013-11-12 Ethicon, Inc. Surgical fasteners, applicator instruments, and methods for deploying surgical fasteners
US8894669B2 (en) 2009-05-12 2014-11-25 Ethicon, Inc. Surgical fasteners, applicator instruments, and methods for deploying surgical fasteners
US8728098B2 (en) 2009-05-12 2014-05-20 Ethicon, Inc. Surgical fasteners, applicator instruments, and methods for deploying surgical fasteners
US8728099B2 (en) 2009-05-12 2014-05-20 Ethicon, Inc. Surgical fasteners, applicator instruments, and methods for deploying surgical fasteners
US8292076B2 (en) 2010-06-22 2012-10-23 Ethicon, Inc. Sealed pouches for medical devices having textured opening flanges and methods therefor
USD641466S1 (en) 2010-09-15 2011-07-12 Ethicon, Inc. Medical device holster
US8413810B2 (en) 2010-09-15 2013-04-09 Ethicon, Inc. Packages for medical devices and methods therefor

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AU2014342636A1 (en) 2016-05-05
JP2016539759A (ja) 2016-12-22
MX2016005777A (es) 2016-08-19
RU2016122047A3 (fr) 2018-06-27
RU2695559C2 (ru) 2019-07-24
EP3065665A1 (fr) 2016-09-14
RU2016122047A (ru) 2017-12-11
WO2015065903A1 (fr) 2015-05-07
IL244908A0 (en) 2016-05-31
AU2014342636B2 (en) 2019-03-07
BR112016009883A8 (pt) 2017-09-19
KR102270343B1 (ko) 2021-06-30
CN106061426A (zh) 2016-10-26
KR20160083053A (ko) 2016-07-11
BR112016009883B1 (pt) 2021-12-28
CN106061426B (zh) 2018-11-09
JP6509889B2 (ja) 2019-05-08
US20150122681A1 (en) 2015-05-07
BR112016009883A2 (fr) 2017-08-01
US9265578B2 (en) 2016-02-23
CA2929093A1 (fr) 2015-05-07

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